Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs143046984 | 0.790 | 0.080 | 14 | 70937529 | intron variant | -/A | delins | 4.2E-02 | 9 | ||
rs202110856 | 0.790 | 0.080 | 5 | 96794169 | intron variant | -/C | delins | 2.1E-05 | 9 | ||
rs377429877 | 0.776 | 0.080 | 13 | 33518027 | intron variant | -/TAA | delins | 6.0E-02 | 10 | ||
rs727502902 | 0.882 | 0.080 | 7 | 140753338 | inframe insertion | -/TAG | delins | 4.0E-06 | 4 | ||
rs121913289 | 1.000 | 0.080 | 10 | 87958013 | frameshift variant | A/- | delins | 4 | |||
rs16892766 | 0.716 | 0.240 | 8 | 116618444 | intergenic variant | A/C | snv | 9.3E-02 | 18 | ||
rs6058093 | 0.776 | 0.080 | 20 | 34625392 | intron variant | A/C | snv | 0.55 | 12 | ||
rs1057519939 | 0.776 | 0.160 | 3 | 179203763 | missense variant | A/C | snv | 10 | |||
rs1566734 | 0.807 | 0.120 | 11 | 48123823 | missense variant | A/C | snv | 0.17 | 0.15 | 10 | |
rs9924886 | 0.776 | 0.080 | 16 | 68710036 | intron variant | A/C | snv | 0.25 | 10 | ||
rs10911251 | 0.790 | 0.080 | 1 | 183112059 | intron variant | A/C | snv | 0.37 | 9 | ||
rs16973225 | 0.790 | 0.080 | 15 | 81937658 | intron variant | A/C | snv | 7.4E-02 | 9 | ||
rs2184857 | 0.790 | 0.080 | 1 | 239918447 | upstream gene variant | A/C | snv | 0.45 | 9 | ||
rs6720296 | 0.790 | 0.080 | 2 | 45181130 | intron variant | A/C | snv | 0.52 | 9 | ||
rs73975588 | 0.790 | 0.080 | 17 | 913501 | intron variant | A/C | snv | 9.9E-02 | 9 | ||
rs1057519928 | 0.807 | 0.200 | 3 | 179221147 | missense variant | A/C | snv | 8 | |||
rs719725 | 0.827 | 0.080 | 9 | 6365683 | intergenic variant | A/C | snv | 0.34 | 7 | ||
rs587780424 | 3 | 12433975 | missense variant | A/C | snv | 1 | |||||
rs1057520002 | 0.695 | 0.360 | 17 | 7674242 | missense variant | A/C;G | snv | 20 | |||
rs11150038 | 0.790 | 0.080 | 16 | 78042662 | intron variant | A/C;G | snv | 10 | |||
rs17102823 | 0.776 | 0.080 | 14 | 34894698 | intergenic variant | A/C;G | snv | 10 | |||
rs281875324 | 1.000 | 0.120 | 18 | 51065456 | missense variant | A/C;G | snv | 3 | |||
rs113488022 | 0.351 | 0.840 | 7 | 140753336 | missense variant | A/C;G;T | snv | 4.0E-06 | 490 | ||
rs1057519975 | 0.649 | 0.480 | 17 | 7675209 | missense variant | A/C;G;T | snv | 34 | |||
rs121913274 | 0.645 | 0.320 | 3 | 179218304 | missense variant | A/C;G;T | snv | 33 |